Allele Registry

Canonical Allele Identifier: PA2579980496

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000445412

ClinVar Variation:

393450

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Glu339Gly	CA16609267 NM_000162.5:c.1016A>G